Porphyria Cutanea Tarda
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
30
|
39
|
0.900 |
None |
0.988 |
85 |
26
|
1976 |
2019 |
Hepatoerythropoietic Porphyria
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
3
|
7
|
0.500 |
None |
0.929 |
28 |
7
|
1981 |
2019 |
Malignant Head and Neck Neoplasm
|
disease |
Neoplasms
|
Neoplastic Process
|
767
|
118
|
0.310 |
None |
1.000 |
1 |
|
2011 |
2011 |
Neck Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
132
|
1
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Cancer of Head
|
disease |
Neoplasms
|
Neoplastic Process
|
35
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Cancer of Neck
|
disease |
Neoplasms
|
Neoplastic Process
|
25
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Upper Aerodigestive Tract Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
24
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Head and Neck Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
124
|
11
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Head Neoplasms
|
group |
Neoplasms
|
Neoplastic Process
|
24
|
|
0.300 |
None |
1.000 |
1 |
|
2011 |
2011 |
Familial porphyria cutanea tarda
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
2
|
6
|
0.200 |
None |
0.912 |
34 |
4
|
1980 |
2019 |
Porphyrias, Hepatic
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
7
|
|
0.200 |
None |
1.000 |
1 |
|
1984 |
1984 |
Porphyria Cutanea Tarda, Type I
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
1
|
1
|
0.110 |
None |
1.000 |
1 |
1
|
1989 |
1989 |
Disorders of Porphyrin Metabolism
|
group |
Nutritional and Metabolic Diseases
|
Disease or Syndrome
|
26
|
7
|
0.100 |
None |
1.000 |
17 |
1
|
1986 |
2019 |
Prader-Willi Syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
Disease or Syndrome
|
185
|
8
|
0.100 |
None |
0.933 |
15 |
|
1992 |
2018 |
Septicemia
|
disease |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
1285
|
141
|
0.100 |
None |
0.857 |
14 |
|
2013 |
2019 |
Sepsis
|
disease |
Pathological Conditions, Signs and Symptoms; Infections
|
Disease or Syndrome
|
1453
|
144
|
0.100 |
None |
0.857 |
14 |
|
2013 |
2019 |
Russell-Silver syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Disease or Syndrome
|
104
|
12
|
0.100 |
None |
0.917 |
12 |
|
1995 |
2019 |
Familial (FPAH)
|
disease |
|
Disease or Syndrome
|
1075
|
276
|
0.100 |
None |
0.900 |
10 |
|
1985 |
2012 |
Leukemia, Myelocytic, Acute
|
disease |
Neoplasms
|
Neoplastic Process
|
3111
|
6892
|
0.100 |
None |
1.000 |
1 |
2
|
2017 |
2017 |
Onycholysis
|
disease |
Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
15
|
|
0.100 |
None |
|
0 |
|
|
|
Facial Hypertrichosis
|
phenotype |
Skin and Connective Tissue Diseases
|
Finding
|
8
|
2
|
0.100 |
None |
|
0 |
|
|
|
Alopecia
|
disease |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Disease or Syndrome
|
491
|
375
|
0.100 |
None |
|
0 |
|
|
|
Cirrhosis
|
disease |
Pathological Conditions, Signs and Symptoms
|
Disease or Syndrome
|
919
|
110
|
0.100 |
None |
|
0 |
|
|
|
Fragile skin
|
phenotype |
|
Finding
|
26
|
5
|
0.100 |
None |
|
0 |
|
|
|
Thin skin
|
phenotype |
|
Finding
|
77
|
4
|
0.100 |
None |
|
0 |
|
|
|